Osteoarthritis (OA) is one of the most frequent musculoskeletal disorders and represents the main indication for total joint arthroplasty. Multipotent mesenchymal stromal cells (MSCs) can be easily isolated and culture expanded from bone marrow aspirates and provide an excellent source of progenitor cells for cell-based regeneration strategies due to their ex vivo differentiation and proliferation capacity. Although there are hints that MSCs derived from OA patients may exhibit altered function the role of MSCs with respect to disease development and progression of OA is not clearly understood to date. To assess whether advanced-stage OA affects MSCs' suitability for musculoskeletal regenerative therapy, in the present study, we compare proliferation and differentiation potential of MSCs from osteoarthritic versus healthy donors.
Clinical data (range of motion of lower limb joints, sociodemographic score dataset, WOMAC score, EQ-5D score, Harris Hip Score, radiological evaluation (OA group only), routine laboratory parameters, and bone metabolism parameters) Osteogenic, chondrogenic, and adipogenic differentiation is proofed qualitatively by cell staining osteogenic, chondrogenic and adipogenic marker gene expression analysis using quantitative real-time RT-PCR cell-specific alkaline phosphatase (ALP) activity assay large-scale gene expression profile Fluorescence-activated cell sorting (FACS)- CD44, CD105 (SH2; endoglin), CD106 (vascular cell adhesion molecule; VCAM-1), CD166, CD29, CD73 (SH3 and SH4), CD90 (Thy-1), CD117, STRO-1 and Sca-1 \[%\]
Study Type
OBSERVATIONAL
Enrollment
30
University Hospital Dresden, Orthopaedic Department
Dresden, Germany
Global Gene expression profile of bone marrow-derived mesenchymal stromal cells from osteoarthritic versus healthy donors
Time frame: after msc isolation
Flow cytometric analysis of cell surface antigens, Alkaline phosphatase activity, DNA content as measure for cellular proliferation
Time frame: variable 2 days up to 21 days after msc cultivation
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